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I'm hoping that since she is younger than me that she will heal faster and wont have any other problems afterwards. She has already been told that her only option is surgery, so our appt on Monday is simply to go over her MRI and to discuss how severe it is and what he would like to do and when. My appt with him, is to set up another Discography for the L4-L5 level, to see if we need to fuse that level now as well and to also go over this "partial" fusion word on the report and what does that mean. I live 20 mins outside of DC and i'm just so tempted to take my venting to the "Hill" about how its completely ridiculous for us CP patients to have to suffer and be afraid to ask for relief so we can function like normal human's do. 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I told her last week to call the oncall doc, which she did, however he completely dismissed her pain and told her to take aleve or to go to the ER. So since then she has been too afraid to call for anything. So today she called me again in tears and this time I was Ped because she didnt want to call the Doc's for fear they would tell her the same thing. So I got on the phone and left a message for our surgeon's nurse, basically telling her that my daughter was experiencing intense pain and that when she called in last week she was told to take aleve and therefore she has been too afraid to call in to ask for anything else, so she has been suffering for a week and could they please call something in for her, to get her through until Monday's appt. Our nurse called me back and unfortunately I missed the call, but she left a message saying that she was soooooo sorry that she was told to take aleve last week, and they would most definatley call something in for her, that they didnt realize how much pain she was in because the oncall doc failed to say anything about her calling in tears last week, that it would be handled and for us to both come at the same time on Monday and again she apologized profusely and said she would get in touch with my daughter immedia 1000 tley to get a pharmacy number to call her something in. Dont get me wrong I absolutley love my surgeon and his nurse, they are wonderful people, its the other doc's in the practice that I cant stand. They did the same thing to me 5 months post op from my fusion when I had called in one night and I got the SAME oncall doc, and instead of calling in what I had been taking, he wanted me to stop that med completely and he wanted to switch me to what he wanted. I told him straight up, that I was not his patient, that he knew nothing at all about me or my history and had no right stopping any of my meds and switching them without the consent of my surgeon. I guess I was right, and he realized that and kept me on what I was taking. When I saw my surgeon the next time I had told him about the conversation and he said that it should have never happened, that nothing should be changed without his consent and that if the Doc had any concerns, he should have called something in to get me through the night until the next day and then had him handle it from there. He said he was going to discuss it with the other doc, but I guess its still happening, because he dismissed my daughters pain. I explained to my daughter that she should never have to be afraid to ask for something for pain from her doctor's office and that it really ticks me off that patients, including myself are so fearful of being labeled because we do ask. This is really begining to irritate me now. At first I wouldnt say anything and I would suffer through it, then I got to where I would just come out and ask for something, if I was told no, then I would look for another doctor, but then your labeled yet again as doctor shopping. Well yes, of course i'm doctor shopping, but its not to get prescribed meds from each and everyone at the same time, it is to find ONE doctor that is willing to treat my pain with whatever works. This is just getting ridiculous now that patients are really suffering from debilitating pain because there are idiots out there that want to enjoy a night of euphoria, they are taking away from us, the people that truly need the med. Its not that we WANT the med, we NEED it to function. What they take for granted and dont even think about on a daily basis, we struggle to do, suffering the consequences of pain afterwards. Then you have the "good" doctors that are willing to treat patients in pain with strong meds and for long term, and they end up getting locked up because street junkies go in and fake they are sick, or the DEA sends in a dummy patient. I would have to say that most of the docs that are treating pain patients now almost 95% of the time want to constantly inject you even after you've been through them and its been found not to work. So once again we agree to be injected, even though for some it causes more pain on top of what we already deal with, just so we can get medication to control our pain. Patients will do anything just to get decent care and it sickens me that we have to be subjected to treatments that have failed in the past just to walk about of an office with a 30 day script. I'm seeing this new PM doc now that wants to inject me every which way, and of course I agree'd to it, but I agree'd for two reasons. One was because I want to give him a chance to see if HIS way works, but I also agree'd to it so that I could get the meds that work for my pain. The truth of the matter is after being injected now for 2 yrs by 2 different docs, this is probably not going to work, although I am really trying to have a positive attitude. I am very thrilled about the aqua-therapy though, which has not been tried yet and i'm anxious to see how that works, but since i've had my fusion several other problems having to deal with pain are now apart of my life, so what was just a lumbar problem, has now turned into sciatic pain, osteopenia, muscle and nerve damage, a failing L4-L5 level, a dragging leg and much more pain than I ever had before 1000 my fusion. I just feel broken and i'm so tired of fighting to get the pain control that I feel I deserve and that I shouldnt have to be so afraid to ask for and now i'm so worried about my daughter now and her having to go through the same crap. I'm hoping that since she is younger than me that she will heal faster and wont have any other problems afterwards. She has already been told that her only option is surgery, so our appt on Monday is simply to go over her MRI and to discuss how severe it is and what he would like to do and when. My appt with him, is to set up another Discography for the L4-L5 level, to see if we need to fuse that level now as well and to also go over this "partial" fusion word on the report and what does that mean. I live 20 mins outside of DC and i'm just so tempted to take my venting to the "Hill" about how its completely ridiculous for us CP patients to have to suffer and be afraid to ask for relief so we can function like normal human's do. To let them know that I find it disgusting that patients with medical records, MRI's, Ct scans, xrays & discography's, ect that PROVE that there is a problem that does cause severe pain should have to even be questioned about treating they're pain, the proof is on paper, in pictures and is in black and white, provide this person the pain relief they need and stop treating them like a street junkies. Worry about the people that dont have proof there is a problem and treat the people that have proof with some respect. I dont know maybe i'll write a letter to my Congressman to let him know how I feel about all this. Thanks for letting me vent, Lisa
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Er place (drank a few glasses of wine there).and then things really got heated up. At that point I was kicking myself 'cuz knew if I took the V I was not giving it enough time to effectively get in my system, but I went for it anyway, taking about 75mg (chewed it up and let it melt under my tongue). We proceeded to some very heavy foreplay (she's VERY passionate), and it was all I could do to keep those nagging self doubts of perfomance anxiety under control. To make a long story short, we wound up making great love for a good long while, actually in 2 separate sessions (about an hr apart). There were a couple of periods in there where I was not as hard as I wanted to be, but I didn't panic, and lo and behold my erection came back, although not *steel hard* as many on this board have described. I don't know whether the V was doin' it's thing or not, since I violated 2 of the taboos of V use: 1 I didn't take it on an empty stomach ,and, 2 I did not allow the 1/2 hr -1 hr for it to get in my system f generic viagra viagrageneric
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Some suggestions from my own experience: first, you must eat right--veggies, non-processed foods, whole wheat, fruits, nuts, etc. At age 63, unlike at age 20, you have to tilt the scales in your favor, and eating smaller, healthier meals is a must. Second, you must exercise regularly. This will, in itself, boost low testosterone levels. Join a gym and get out the weights, get on the machines, and exercise rigorously for 45 minutes three times a week at least. This has done wonders for my sex life. It gets the blood flowing again in vital places and gets you stamina up so you aren't winded and pooped out when you are exerting yourself during sex. You have the muscles to perform. Try Kegel exercises, too. You will find you can last much longer and enjoy sex much more with a good regular program of exercise. Third, you must get off the drugs. Lipitor and other drugs are detrimental to your overall health and sex life. Get your weight on down, get off the drugs, and you will have increased energy. Finally, you mi| Viagra overnight delivery to canada |
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I take ultram er for chronic back pain, it works very well. i am also blessed with severe incontinence. My dr. gave me imipramine. Everything i have read about it says you should take the two together. I don't know what to think of this and am tempted to question her. Although I hate to question my doctor, surely she knows this. Comments?
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Some suggestions from my own experience: first, you must eat right--veggies, non-processed foods, whole wheat, fruits, nuts, etc. At age 63, unlike at age 20, you have to tilt the scales in your favor, and eating smaller, healthier meals is a must. Second, you must exercise regularly. This will, in itself, boost low testosterone levels. Join a gym and get out the weights, get on the machines, and exercise rigorously for 45 minutes three times a week at least. This has done wonders for my sex life. It gets the blood flowing again in vital places and gets you stamina up so you aren't winded and pooped out when you are exerting yourself during sex. You have the muscles to perform. Try Kegel exercises, too. You will find you can last much longer and enjoy sex much more with a good regular program of exercise. Third, you must get off the drugs. Lipitor and other drugs are detrimental to your overall health and sex life. Get your weight on down, get off the drugs, and you will have increased energy. Finally, you mi| Viagra overnight delivery to canada |
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P.E only 20 :( Alpha blockers and viagra Hello World! I have been reading as much as I can about penile implants. I have been reading this post and thought I might chime in, ask a question and find some support. So here it goes, (art most of this will be review for you). I am 39 years old, not a young guy but not old either, in good health, married and currently experiencing ED. A few weeks ago I had a medical emergency. I had a priapism (erection lasting longer than four hours) due to a drug (trazadone) reaction. Irrigation and aspiration did not work so the Uro put in a winter shunt to relieve the blood. Since then my penis has been “puffier” than normal and I have not had a full erection. My erections are 10 to 15 percent of what they were and they are not on auto-pilot anymore (morning wood) I really have to work at it (even with Viagra and cialis which I don’t believe have any effect at all except maybe psychologically) and they only last a few minutes if at all. The Uro who treated me said that there is permanent damage to the corpora. OK, that being said, I have asked plenty of questions on other forums and from others who have had an implant (thank you Art). But after reading all the forums (I mean a lot of them, to the point of obsession) I have found a few things to be true. There are always the disgruntled few (and rightly so, about botched operations and loss of length). There are those who have had it done for medical reasons (cancer, leaky veins/plumping). There are those who have had it done for traumatic reasons (drug reaction (me), accident/injury). And the majority of all these posts end up with pretty much the same ending sentence, ” I would have the implant done again tomorrow if I had to, I wish I did it earlier.” So taking the risks into consideration 1) infection, which is about 3% of the cases a number I can live with I think the odds are in the patients favor 2) Loss of Length, better then a total loss of sex, and 3) possible hardware malfunction, I have a hardware malfunction now and it’s bio-mechanical. (Please keep in mind these are as I see it, your mileage may vary). When was your tipping point? When did you stop tilting at windmills? Do you look back with hind sight and say ok I should have taken this route months or even years ago? flu treatment in apothekendoxycycline 20 mg price of My sister's husband told me about a pill called Macaenhancer which he LOVES! He says it not only increased his sperm count (they're trying to have a baby), but also his erection size and drive. If it worked for my sister's husband, it could work for you. Lowest price viagra check money order
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I'm in a monogamous relationship for 4 years. We are in very good shape for men in our 60's and there are no health issues. For the most part our sex lives are pretty good in terms of frequency (several x's a week) but it is becoming too routine. In this respect we're probably no different than heterosexual couples. When we first started out the sex was fantastic and we were both eager to please one another. I have a high libido but I don't pressure him for sex. Anyway, I seem to be the one accomodating each time we have sex concerning the time of day and position, etc. I've mentioned that we should try new ways of pleasing each other and I have only been successful a handful of times in the last 4 years. When I ask for something different (nothing kinky - but maybe I should ask) he says it doesn't make him feel good and he doesn't like that position cause it does nothing for him (even though it would drive me nuts). I tell him certain things really turn me on but he doesn't pick up on this. I've asked if he's lost interest in me and he says no. It just doesn't feel like he's totally into the sex part like before. Maybe he's not feeling good about himself? Or things have changed for him but he won't say why? I've even sent him many articles to read about the joy of sex and how to be more creative in the bedroom so it spices things up a bit but nothing ever happens. I tell him how much he turns me on and praise him a lot but it still ends up the same way in the bedroom. We've watched one porno movie together so he could get an idea of the myriad of things possible in the bedroom and that didn't work either. I don't want to go outside the relationship - that just seems to always lead to more problems and I don't think it's healthy. I really am grateful for the intimate time we spend together. When I do bring up changing things he replys that sex isn't all there is. We're both getting older. Maybe that's it? Any suggestions? I don't understand how you can be really sexual in the beginning of a relationship and then become sort of only one way later? Thanks, Tom
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Need some advice while I am here, so will try and keep it short and sweet. Basically 2 1/2 years ago July 06 I fell down a flight of outdoor cement steps at home and shattered right leg tib/fib open bone blood all over step. Had metal rod put in (also broke left index finger), healing took 3 months to get a weight baring, had 4 other surgeries since 2 finger, 2 leg plus they put a Greenfield filter in me due to me being a lil overweight and not getting the weight baring status right away. While I was being treated the whole first year through the surgeries and original PT I was on either Vicodin or Percocet, both which got me through the horror - they used a shot of morphine on me when the surgeon got the bright idea to manually manupulate my index finger in ER to try and get it too move again - well he rebroke it doing so and it doesn't move now is stuck and no one seemed to think I had a malpractice case. anyone thankfully other than being non-useful to me and causing me annoyance as in not being able to open things easily and use my hand to grip, the finger barely causes me pain - every now and then a light throb, especially when weather is bad or changes. Leg however is a totally different story. Was with a PM Dr. for over 6 months he had me on Opana ER, Cymbalta and a muscle relaxer. The pain was never fully taken away from this combo, but I tolerated it for the most part but he also had me signed out of work on FMLA and I did 3x a week PT. During that time a foot dr. discovered I had a severe fallen arch that no one had caught yet, needless to say the medication made me a zombie and I became so unmotivated I lost my life to the point my family had to get involved and go with me six months down the line after I was losing my job, to ask this Dr. when does he stop just writing scripts and try and figure out why I am in so much pain. Needless to say Dr. got pissed off and then just signed me back in, went for another opinion and that Dr. said I shouldn't return to work and the difference in opinion and Metlife not granting me long term disability from short term disability ended with me losing my job. Second opinion did an EMG and MRI, they found slight to moderate nerve damage in leg and felt in the end it could be the regeneration of the nerves at this point causing me the discomfort and pain. I still limp however and now my knee seems out in my good (left leg) making it hard to get up from a sitting position. I am so fustrated and sick of Drs. I am paying through the nose for Cobra thinking I needed it, saw a neurologist who really just sent me to a new pain management Dr. who from first impression saw me for 15 mins and sent me out with a book of perscriptions including what seems like duplicates: ultram er, tramadol, methadone, celebrex and pretiq. I am so afraid to fill these at this point since the last set just made me a zombie and made me never le 1000 ave my house, sleep all day and not even have motivation to see friends and family. I do not want to go back to that state again. I have been up all night because I am having a bad attack of pain that feels like ants with razor sharp claws are crawling up and down my lower leg at a very slow speed to induce absolute torture to me, not allowing me to get comfortable at all. Overall since I had stoped the medication from the first bout and only took left over vicodins as needed - maybe every few days when the pain was bad - I got more done during that month, was so much of a happier person, getting back to my old self and getting stuff done with less pain - even my friends and family noticed the huge improvement. Yet tell a PM that, and for some odd reason they won't perscribe the one thing that actually works for me, but they'll give me all these crazy pills like methadone and opana. I just can't understand it. I have no history at all of addiction and I just don't trust doctors anymore. I don't know if I should fill this new set of scripts (luckily my best friend is a pharmacist, but she said the trimadal and the ultram was the same drug, which makes me wonder why do I need both? and then makes me question if this doctor is even good and doing the right thing) and just see if they work, or just try and go see more doctors. 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I would like everyone to please help to support the world of mma by purchasing the upcoming UFC 44 UNDISPUTED event. This will be an outstanding event that will have champion vs champion. When the current champion Tito Ortiz takes on Interim champion Randy Couture. Together we can all get this sport the attention that it needs to make it into the main stream. http://ourworld.cs.com/sabo911/ufc44_360X60_soon.gif ------------------ WHAT'S THE BEST MMA FANTASY BOARD ON THE NET ? url="http://ultmmafantasy.proboards15.com/index.cgi"http://ultmmafantasy.proboards15.com/index.cgi/url Play by play, promo's, interviews. Up to date real MMA NEWS and TRAINING SECTION. CHECK IT OUT This message has been edited by STORM911 (edited 09-21-2003).
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I'm sure this has been asked before.so please forgive me for being repetative. Tomorrow I'm going to my MD for a complete physical at which time I'll tell him to get me some Viagra or similar drug. Yeah, it's embarrasing.but so is failing my wife for many months and my self esteem. I mentioned to my doctor awhile back that I was "having problems" and he told me it was probably depression and not to worry about it.well, it is obvious that his advice was wrong, so tomorrow I'm insisting on chemical assistance for this problem. Here's where you guys come in. What should I ask or know before I see him? I know theres a couple other drugs out there aside from Viagra.and I understand every person reacts differently for each one. Any advice you guys can offer? thanks!
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